Reference/ChEBI CHEBI 16015
type: UnificationXref
id: CHEBI:16015
db: ChEBI

Reference/ChemSpider 30572
type: UnificationXref
id: 30572
db: ChemSpider

Acetyl-CoA
type: SmallMoleculeReference
xref: Reference/BioCyc ACETYL-COA
xref: Reference/PubChem-compound 444493
xref: Reference/HMDB HMDB0001206
xref: Reference/ChemSpider 392413
xref: Reference/CAS 72-89-9
xref: Reference/ChEBI CHEBI 15351
xref: Reference/KEGG Compound C00024
chemical formula: C23H38N7O17P3S
molecular weight: 809.1258
structure: ChemicalStructure/PW C000940

Compound/PW C007838/Stoichiometry/1.0
type: Stoichiometry
physical entity: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate
stoichiometric coefficient: 1.0

Reference/ChemSpider 937
type: UnificationXref
id: 937
db: ChemSpider

Phospho-N-acetylmuramoyl-pentapeptide-transferase
type: ProteinReference
xref: Reference/UniProt D6D050

Bacterial polymer biosynthesis proteins, WecB/TagA/CpsF family
type: ProteinReference
xref: Reference/UniProt D6D5U2

Minor fimbrium subunit Mfa1 C-terminal domain-containing protein
type: ProteinReference
xref: Reference/UniProt D6D610

dTDP-D-glucose
type: SmallMolecule
entity reference: dTDP-D-glucose

[Ribosomal protein bS18]-alanine N-acetyltransferase
type: ProteinReference
xref: Reference/UniProt D6D4W5

ChemicalStructure/PW C001420
type: ChemicalStructure
structure format: SMILES
structure data: O

Bacteroides xylanisolvens XB1A
type: BioSource
xref: Reference/TAXONOMY 657309

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

Membrane protein involved in the export of O-antigen and teichoic acid
type: ProteinReference
xref: Reference/UniProt D6CYA4

Reference/ChemSpider 50
type: UnificationXref
id: 50
db: ChemSpider

Compound/PW C040034/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen Ion
stoichiometric coefficient: 1.0

ChemicalStructure/PW C042658
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C042652
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C042654
type: ChemicalStructure
structure format: SMILES

Reference/UniProt D6D050
type: UnificationXref
id: D6D050
db: UniProt

Reference/ChEBI CHEBI 16264
type: UnificationXref
id: CHEBI:16264
db: ChEBI

Compound/PW C007839/Stoichiometry/1.0
type: Stoichiometry
physical entity: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
stoichiometric coefficient: 1.0

Compound/PW C000095/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Glutamic acid
stoichiometric coefficient: 1.0

Reference/CAS 528-04-1
type: UnificationXref
id: 528-04-1
db: CAS

Reference/ChEBI CHEBI 68492
type: UnificationXref
id: CHEBI:68492
db: ChEBI

Reference/PubChem-compound 6816
type: UnificationXref
id: 6816
db: PubChem-compound

Reference/PubChem-compound 51
type: UnificationXref
id: 51
db: PubChem-compound

Reference/ChemSpider 559142
type: UnificationXref
id: 559142
db: ChemSpider

Reference/UniProt D6D610
type: UnificationXref
id: D6D610
db: UniProt

Protein/55810/Stoichiometry/4.0
type: Stoichiometry
physical entity: Aspartate/tyrosine/aromatic aminotransferase
stoichiometric coefficient: 4.0

Compound/PW C001024 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: dTDP-D-glucose
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00459
type: UnificationXref
id: C00459
db: KEGG Compound

Reference/ChemSpider 388455
type: UnificationXref
id: 388455
db: ChemSpider

Compound/PW C000940/Stoichiometry/1.0
type: Stoichiometry
physical entity: Acetyl-CoA
stoichiometric coefficient: 1.0

Reference/CAS 365-08-2
type: UnificationXref
id: 365-08-2
db: CAS

Reference/PubChem-compound 1038
type: UnificationXref
id: 1038
db: PubChem-compound

Reference/GENE ONTOLOGY GO 0005829
type: UnificationXref
id: GO:0005829
db: GENE ONTOLOGY

Oxoglutaric acid
type: SmallMoleculeReference
xref: Reference/CAS 328-50-7
xref: Reference/PubChem-compound 51
xref: Reference/BioCyc 2-KETOGLUTARATE
xref: Reference/HMDB HMDB0000208
xref: Reference/ChEBI CHEBI 30915
xref: Reference/KEGG Compound C00026
xref: Reference/ChemSpider 50
chemical formula: C5H6O5
molecular weight: 146.02153
structure: ChemicalStructure/PW C000134

Secondary Metabolites: Methylerythritol Phosphate and Polyisoprenoid Biosynthesis
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway479682
pathway component: SubPathwayInteraction479682
xref: Reference/SMPDB SMP0000974
xref: Reference/PathWhiz PW000958
name: SubPathway

Reference/PubChem-compound 64968
type: UnificationXref
id: 64968
db: PubChem-compound

Reference/ChemSpider 393240
type: UnificationXref
id: 393240
db: ChemSpider

Reference/PathWhiz PW000958
type: UnificationXref
id: PW000958
db: PathWhiz

N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol
type: SmallMolecule
entity reference: N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol

Reference/KEGG Compound C00105
type: UnificationXref
id: C00105
db: KEGG Compound

dTDP-thomosamine
type: SmallMolecule
entity reference: dTDP-thomosamine

Reference/PubChem-compound 6030
type: UnificationXref
id: 6030
db: PubChem-compound

Reference/PubChem-compound 6031
type: UnificationXref
id: 6031
db: PubChem-compound

Reference/HMDB HMDB0012306
type: UnificationXref
id: HMDB0012306
db: HMDB

Reference/PubChem-compound 164628
type: UnificationXref
id: 164628
db: PubChem-compound

Pyrophosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Pyrophosphate

Acetyl-CoA
type: SmallMolecule
entity reference: Acetyl-CoA

Reference/ChemSpider 58493
type: UnificationXref
id: 58493
db: ChemSpider

Reference/KEGG Compound C00103
type: UnificationXref
id: C00103
db: KEGG Compound

Reference/ChemSpider 1010
type: UnificationXref
id: 1010
db: ChemSpider

Thymidine 5'-triphosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Thymidine 5'-triphosphate

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 439165
type: UnificationXref
id: 439165
db: PubChem-compound

ChemicalStructure/PW C000201
type: ChemicalStructure
structure format: SMILES

Reference/BioCyc PPI
type: UnificationXref
id: PPI
db: BioCyc

Compound/PW C000987/Stoichiometry/1.0
type: Stoichiometry
physical entity: dTDP
stoichiometric coefficient: 1.0

ReactionCatalysis1073233
type: Catalysis
controller: dTDP-4-dehydro-6-deoxy-D-glucose transaminase
controlled: 2.6.1.59
control type: ACTIVATION

Reference/ChemSpider 144320
type: UnificationXref
id: 144320
db: ChemSpider

ReactionCatalysis1073234
type: Catalysis
controller: dTDP-glucose pyrophosphorylase
controlled: 2.7.7.24
control type: ACTIVATION

Reference/UniProt D6D5U2
type: UnificationXref
id: D6D5U2
db: UniProt

ReactionCatalysis1073231
type: Catalysis
controller: Minor fimbrium subunit Mfa1 C-terminal domain-containing protein
controlled: 2.4.1.325
control type: ACTIVATION

dTDP
type: SmallMoleculeReference
xref: Reference/CAS 491-97-4
xref: Reference/ChemSpider 144320
xref: Reference/PubChem-compound 164628
xref: Reference/KEGG Compound C00363
xref: Reference/ChEBI CHEBI 18075
xref: Reference/HMDB HMDB0001274
xref: Reference/BioCyc TDP
chemical formula: C10H16N2O11P2
molecular weight: 402.02292
structure: ChemicalStructure/PW C000987

ReactionCatalysis1073232
type: Catalysis
controller: [Ribosomal protein bS18]-alanine N-acetyltransferase
controlled: 2.3.1.210
control type: ACTIVATION

Amino Sugar and Nucleotide Sugar Metabolism I
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway479681
pathway component: SubPathwayInteraction479681
xref: Reference/PathWhiz PW000886
xref: Reference/SMPDB SMP0000905
name: SubPathway

Galactose Degradation/Leloir Pathway
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway479683
pathway component: SubPathwayInteraction479683
xref: Reference/SMPDB SMP0000903
xref: Reference/PathWhiz PW000884
name: SubPathway

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

ReactionCatalysis1073235
type: Catalysis
controller: dTDP-glucose pyrophosphorylase 2
controlled: 2.7.7.24
control type: ACTIVATION

Glucose 1-phosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Glucose 1-phosphate

Reference/CAS 59-56-3
type: UnificationXref
id: 59-56-3
db: CAS

Reference/HMDB HMDB0000208
type: UnificationXref
id: HMDB0000208
db: HMDB

Cytosol
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005829

Reference/ChemSpider 388311
type: UnificationXref
id: 388311
db: ChemSpider

Compound/PW C000170 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Pyrophosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0001423
type: UnificationXref
id: HMDB0001423
db: HMDB

L-Glutamic acid
type: SmallMolecule
entity reference: L-Glutamic acid

ChemicalStructure/PW C000134
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)CCC(=O)C(O)=O

Reference/HMDB HMDB0012307
type: UnificationXref
id: HMDB0012307
db: HMDB

Reference/ChEBI CHEBI 30915
type: UnificationXref
id: CHEBI:30915
db: ChEBI

Reference/PathWhiz PW460124
type: UnificationXref
id: PW460124
db: PathWhiz

Uridine diphosphate-N-acetylglucosamine
type: SmallMoleculeReference
xref: Reference/CAS 528-04-1
xref: Reference/PubChem-compound 445675
xref: Reference/HMDB HMDB0000290
xref: Reference/BioCyc UDP-N-ACETYL-D-GLUCOSAMINE
xref: Reference/KEGG Compound C00043
xref: Reference/ChEBI CHEBI 16264
xref: Reference/ChemSpider 393240
chemical formula: C17H27N3O17P2
molecular weight: 607.08154
structure: ChemicalStructure/PW C000196

Uridine 5'-monophosphate
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000288
xref: Reference/CAS 58-97-9
xref: Reference/KEGG Compound C00105
xref: Reference/PubChem-compound 6030
xref: Reference/BioCyc UMP
xref: Reference/ChEBI CHEBI 16695
xref: Reference/ChemSpider 5808
chemical formula: C9H13N2O9P
molecular weight: 324.03586
structure: ChemicalStructure/PW C000194

Compound/PW C042658/Stoichiometry/1.0
type: Stoichiometry
physical entity: dTDP-4-dehydro-6-deoxy-D-glucose
stoichiometric coefficient: 1.0

Reference/UniProt D6D5T2
type: UnificationXref
id: D6D5T2
db: UniProt

Hydrogen Ion
type: SmallMolecule
cellular location: Cytosol
entity reference: Hydrogen Ion

Reference/SMPDB SMP0000974
type: UnificationXref
id: SMP0000974
db: SMPDB

Reference/KEGG Compound C00001
type: UnificationXref
id: C00001
db: KEGG Compound

Glucose-1-phosphate thymidylyltransferase
type: Protein
cellular location: Cytosol
entity reference: Glucose-1-phosphate thymidylyltransferase

Reference/KEGG Compound C00363
type: UnificationXref
id: C00363
db: KEGG Compound

ReactionCatalysis1072931
type: Catalysis
controller: dTDP-glucose 4,6-dehydratase
controlled: 4.2.1.46
control type: ACTIVATION

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
type: SmallMolecule
entity reference: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate

ReactionCatalysis1073229
type: Catalysis
controller: undecaprenyl-phosphate α-N-acetylglucosaminyl transferase
controlled: 2.7.8.33
control type: ACTIVATION

Reference/HMDB HMDB0060081
type: UnificationXref
id: HMDB0060081
db: HMDB

Reference/ChEBI CHEBI 35248
type: UnificationXref
id: CHEBI:35248
db: ChEBI

Reference/ChEBI CHEBI 18361
type: UnificationXref
id: CHEBI:18361
db: ChEBI

ChemicalStructure/PW C042617
type: ChemicalStructure
structure format: SMILES
structure data: CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/COP(O)(O)=O

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate
type: SmallMolecule
entity reference: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate

dTDP-glucose pyrophosphorylase
type: Complex
component stoichiometry: Protein/55818/Stoichiometry/4.0
component: Glucose-1-phosphate thymidylyltransferase

Compound/PW C007839 Periplasmic Space/Stoichiometry/1.0
type: Stoichiometry
physical entity: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
stoichiometric coefficient: 1.0

Reference/BioCyc GLC-1-P
type: UnificationXref
id: GLC-1-P
db: BioCyc

undecaprenyl-phosphate α-N-acetylglucosaminyl transferase
type: Complex
component stoichiometry: Protein/76734/Stoichiometry/2.0
component: Phospho-N-acetylmuramoyl-pentapeptide-transferase

2.4.1.325
type: BiochemicalReaction
participant stoichiometry: Compound/PW C007839/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007838/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000987/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042652/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen Ion
right: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
right: dTDP
spontaneous: false
EC number: 2.4.1.325
left: TDP-Fuc4NAc
left: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate
name: TDP-Fuc4NAc + Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate → Hydrogen Ion + Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate + dTDP
conversion direction: LEFT_TO_RIGHT

Reference/BioCyc GLT
type: UnificationXref
id: GLT
db: BioCyc

dTDP-glucose pyrophosphorylase 2
type: Complex
component stoichiometry: Protein/55818/Stoichiometry/4.0
component: Glucose-1-phosphate thymidylyltransferase
name: SubPathwayInput

Compound/PW C042617/Stoichiometry/1.0
type: Stoichiometry
physical entity: di-trans,octa-cis-undecaprenyl phosphate
stoichiometric coefficient: 1.0

2.4.1.180
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000201/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007838/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042654/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042941/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen Ion
right: Uridine 5'-diphosphate
right: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate
spontaneous: false
EC number: 2.4.1.180
left: N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol
left: UDP-ManNAcA
name: N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol + UDP-ManNAcA → Hydrogen Ion + Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate + Uridine 5'-diphosphate
conversion direction: LEFT_TO_RIGHT

2.7.8.33
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000196/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000194/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042617/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042941/Stoichiometry/1.0
right: N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol
right: Uridine 5'-monophosphate
spontaneous: false
EC number: 2.7.8.33
left: Uridine diphosphate-N-acetylglucosamine
left: di-trans,octa-cis-undecaprenyl phosphate
name: Uridine diphosphate-N-acetylglucosamine + di-trans,octa-cis-undecaprenyl phosphate → N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol + Uridine 5'-monophosphate
conversion direction: LEFT_TO_RIGHT

dTDP-4-dehydro-6-deoxy-D-glucose transaminase
type: Complex
component stoichiometry: Protein/55810/Stoichiometry/4.0
component: Aspartate/tyrosine/aromatic aminotransferase

ReactionCatalysis1073230
type: Catalysis
controller: Bacterial polymer biosynthesis proteins, WecB/TagA/CpsF family
controlled: 2.4.1.180
control type: ACTIVATION

Reference/UniProt D6D5T4
type: UnificationXref
id: D6D5T4
db: UniProt

2.7.7.24
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001024 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001035 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001207 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170 Cytosol/Stoichiometry/1.0
right: Pyrophosphate
right: dTDP-D-glucose
spontaneous: false
EC number: 2.7.7.24
left: Thymidine 5'-triphosphate
left: Glucose 1-phosphate
left: Hydrogen Ion
name: Glucose 1-phosphate + Hydrogen Ion + Thymidine 5'-triphosphate → Pyrophosphate + dTDP-D-glucose
conversion direction: LEFT_TO_RIGHT

2.7.7.24
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001207/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001035/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001024/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: dTDP-D-glucose
right: Pyrophosphate
spontaneous: false
EC number: 2.7.7.24
left: Thymidine 5'-triphosphate
left: Hydrogen Ion
left: Glucose 1-phosphate
name: Glucose 1-phosphate + Hydrogen Ion + Thymidine 5'-triphosphate → Pyrophosphate + dTDP-D-glucose
conversion direction: LEFT_TO_RIGHT

2.6.1.59
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042658/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042942/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134/Stoichiometry/1.0
right: dTDP-thomosamine
right: Oxoglutaric acid
spontaneous: false
EC number: 2.6.1.59
left: L-Glutamic acid
left: dTDP-4-dehydro-6-deoxy-D-glucose
name: L-Glutamic acid + dTDP-4-dehydro-6-deoxy-D-glucose → dTDP-thomosamine + Oxoglutaric acid
conversion direction: LEFT_TO_RIGHT

Compound/PW C001035 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Thymidine 5'-triphosphate
stoichiometric coefficient: 1.0

2.3.1.210
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000940/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042942/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042652/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Coenzyme A
right: TDP-Fuc4NAc
right: Hydrogen Ion
spontaneous: false
EC number: 2.3.1.210
left: dTDP-thomosamine
left: Acetyl-CoA
name: dTDP-thomosamine + Acetyl-CoA → Coenzyme A + Hydrogen Ion + TDP-Fuc4NAc
conversion direction: LEFT_TO_RIGHT

Compound/PW C040034 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen Ion
stoichiometric coefficient: 1.0

Reference/PathWhiz PW000886
type: UnificationXref
id: PW000886
db: PathWhiz

Reference/PathWhiz PW000884
type: UnificationXref
id: PW000884
db: PathWhiz

Reference/KEGG Compound C00010
type: UnificationXref
id: C00010
db: KEGG Compound

Reference/KEGG Compound C00015
type: UnificationXref
id: C00015
db: KEGG Compound

Compound/PW C042941/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol
stoichiometric coefficient: 1.0

Reference/BioCyc TDP
type: UnificationXref
id: TDP
db: BioCyc

Reference/KEGG Compound C00013
type: UnificationXref
id: C00013
db: KEGG Compound

Uridine diphosphate-N-acetylglucosamine
type: SmallMolecule
entity reference: Uridine diphosphate-N-acetylglucosamine

Pyrophosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 644102
xref: Reference/BioCyc PPI
xref: Reference/ChemSpider 559142
xref: Reference/ChEBI CHEBI 18361
xref: Reference/HMDB HMDB0000250
xref: Reference/CAS 14000-31-8
xref: Reference/KEGG Compound C00013
chemical formula: H4O7P2
molecular weight: 177.94322
structure: ChemicalStructure/PW C000170

Uridine 5'-monophosphate
type: SmallMolecule
entity reference: Uridine 5'-monophosphate

dTDP-D-glucose
type: SmallMoleculeReference
xref: Reference/ChemSpider 388455
xref: Reference/KEGG Compound C00842
xref: Reference/PubChem-compound 439324
xref: Reference/HMDB HMDB0001328
xref: Reference/CAS 2196-62-5
xref: Reference/ChEBI CHEBI 35248
xref: Reference/BioCyc DTDP-D-GLUCOSE
chemical formula: C16H26N2O16P2
molecular weight: 564.07574
structure: ChemicalStructure/PW C001024

Reference/HMDB HMDB0001328
type: UnificationXref
id: HMDB0001328
db: HMDB

Reference/HMDB HMDB0001206
type: UnificationXref
id: HMDB0001206
db: HMDB

Reference/GENE ONTOLOGY GO 0005620
type: UnificationXref
id: GO:0005620
db: GENE ONTOLOGY

dTDP-D-glucose
type: SmallMolecule
cellular location: Cytosol
entity reference: dTDP-D-glucose

Hydrogen Ion
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00080
xref: Reference/ChEBI CHEBI 15378
xref: Reference/HMDB HMDB0059597
xref: Reference/PubChem-compound 1038
xref: Reference/ChemSpider 1010
chemical formula: H
molecular weight: 1.007825
structure: ChemicalStructure/PW C040034

Compound/PW C001035/Stoichiometry/1.0
type: Stoichiometry
physical entity: Thymidine 5'-triphosphate
stoichiometric coefficient: 1.0

Phospho-N-acetylmuramoyl-pentapeptide-transferase
type: Protein
entity reference: Phospho-N-acetylmuramoyl-pentapeptide-transferase

ChemicalStructure/PW C001207
type: ChemicalStructure
structure format: SMILES

Membrane protein involved in the export of O-antigen and teichoic acid
type: Protein
entity reference: Membrane protein involved in the export of O-antigen and teichoic acid

[Ribosomal protein bS18]-alanine N-acetyltransferase
type: Protein
entity reference: [Ribosomal protein bS18]-alanine N-acetyltransferase

Reference/KEGG Compound C00026
type: UnificationXref
id: C00026
db: KEGG Compound

Minor fimbrium subunit Mfa1 C-terminal domain-containing protein
type: Protein
entity reference: Minor fimbrium subunit Mfa1 C-terminal domain-containing protein

dTDP
type: SmallMolecule
entity reference: dTDP

Aspartate/tyrosine/aromatic aminotransferase
type: Protein
entity reference: Aspartate/tyrosine/aromatic aminotransferase

Reference/KEGG Compound C00025
type: UnificationXref
id: C00025
db: KEGG Compound

Bacterial polymer biosynthesis proteins, WecB/TagA/CpsF family
type: Protein
entity reference: Bacterial polymer biosynthesis proteins, WecB/TagA/CpsF family

Reference/KEGG Compound C00024
type: UnificationXref
id: C00024
db: KEGG Compound

Thymidine 5'-triphosphate
type: SmallMolecule
entity reference: Thymidine 5'-triphosphate

Thymidine 5'-triphosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00459
xref: Reference/CAS 365-08-2
xref: Reference/ChEBI CHEBI 18077
xref: Reference/ChemSpider 58493
xref: Reference/PubChem-compound 64968
xref: Reference/HMDB HMDB0001342
xref: Reference/BioCyc TTP
chemical formula: C10H17N2O14P3
molecular weight: 481.98926
structure: ChemicalStructure/PW C001035

Glucose-1-phosphate thymidylyltransferase
type: Protein
entity reference: Glucose-1-phosphate thymidylyltransferase

Reference/ChEBI CHEBI 7137
type: UnificationXref
id: CHEBI:7137
db: ChEBI

Compound/PW C042654/Stoichiometry/1.0
type: Stoichiometry
physical entity: UDP-ManNAcA
stoichiometric coefficient: 1.0

Reference/BioCyc TTP
type: UnificationXref
id: TTP
db: BioCyc

UDP-ManNAcA
type: SmallMolecule
entity reference: UDP-ManNAcA
name: SubPathwayOutput

Reference/UniProt D6D4W5
type: UnificationXref
id: D6D4W5
db: UniProt

Compound/PW C000194/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine 5'-monophosphate
stoichiometric coefficient: 1.0

Compound/PW C000201/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine 5'-diphosphate
stoichiometric coefficient: 1.0

Reference/PubChem-compound 53481400
type: UnificationXref
id: 53481400
db: PubChem-compound

TDP-Fuc4NAc
type: SmallMolecule
entity reference: TDP-Fuc4NAc

dTDP-4-dehydro-6-deoxy-D-glucose
type: SmallMolecule
entity reference: dTDP-4-dehydro-6-deoxy-D-glucose

Reference/BioCyc UDP
type: UnificationXref
id: UDP
db: BioCyc

Reference/CAS 328-50-7
type: UnificationXref
id: 328-50-7
db: CAS

Reference/HMDB HMDB0001586
type: UnificationXref
id: HMDB0001586
db: HMDB

Reference/ChEBI CHEBI 1146900
type: UnificationXref
id: CHEBI:1146900
db: ChEBI

Water
type: SmallMolecule
entity reference: Water

ChemicalStructure/PW C001024
type: ChemicalStructure
structure format: SMILES

Reference/UniProt D6D4W8
type: UnificationXref
id: D6D4W8
db: UniProt

Reference/HMDB HMDB0000250
type: UnificationXref
id: HMDB0000250
db: HMDB

Reference/HMDB HMDB0001342
type: UnificationXref
id: HMDB0001342
db: HMDB

ChemicalStructure/PW C000170
type: ChemicalStructure
structure format: SMILES
structure data: OP(O)(=O)OP(O)(O)=O

Reference/CAS 14000-31-8
type: UnificationXref
id: 14000-31-8
db: CAS

Reference/KEGG Compound C00842
type: UnificationXref
id: C00842
db: KEGG Compound

Reference/UniProt D6CYA4
type: UnificationXref
id: D6CYA4
db: UniProt

Reference/BioCyc CO-A
type: UnificationXref
id: CO-A
db: BioCyc

dTDP-glucose 4,6-dehydratase
type: ProteinReference
xref: Reference/UniProt D6D5T4

Reference/KEGG Compound C00043
type: UnificationXref
id: C00043
db: KEGG Compound

Uridine 5'-diphosphate
type: SmallMolecule
entity reference: Uridine 5'-diphosphate

Reference/CAS 72-89-9
type: UnificationXref
id: 72-89-9
db: CAS

Compound/PW C042652/Stoichiometry/1.0
type: Stoichiometry
physical entity: TDP-Fuc4NAc
stoichiometric coefficient: 1.0

Reference/CAS 58-97-9
type: UnificationXref
id: 58-97-9
db: CAS

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

Compound/PW C000196/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine diphosphate-N-acetylglucosamine
stoichiometric coefficient: 1.0

Coenzyme A
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 1146900
xref: Reference/HMDB HMDB0001423
xref: Reference/PubChem-compound 6816
xref: Reference/BioCyc CO-A
xref: Reference/ChemSpider 6557
xref: Reference/CAS 85-61-0
xref: Reference/KEGG Compound C00010
chemical formula: C21H36N7O16P3S
molecular weight: 767.11523
structure: ChemicalStructure/PW C001099

Compound/PW C000170/Stoichiometry/1.0
type: Stoichiometry
physical entity: Pyrophosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000148
type: UnificationXref
id: HMDB0000148
db: HMDB

ChemicalStructure/PW C001035
type: ChemicalStructure
structure format: SMILES

Uridine 5'-diphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17659
xref: Reference/PubChem-compound 6031
xref: Reference/CAS 58-98-0
xref: Reference/HMDB HMDB0000295
xref: Reference/KEGG Compound C00015
xref: Reference/ChemSpider 5809
xref: Reference/BioCyc UDP
chemical formula: C9H14N2O12P2
molecular weight: 404.0022
structure: ChemicalStructure/PW C000201

ChemicalStructure/PW C042942
type: ChemicalStructure
structure format: SMILES

Secondary Metabolites: Enterobacterial Common Antigen Biosynthesis
type: Pathway
pathway order: PathwaySubPathway/479681
pathway order: PathwayEnzymeReaction/6502781
pathway order: PathwaySubPathway/479682
pathway order: PathwayEnzymeReaction/6502782
pathway order: PathwayEnzymeReaction/6502783
pathway order: PathwayEnzymeReaction/6502784
pathway order: PathwayEnzymeReaction/6502774
pathway order: PathwayEnzymeReaction/6502785
pathway order: PathwayEnzymeReaction/6502775
pathway order: PathwayEnzymeReaction/6502778
pathway order: PathwayTransport/6502788
pathway order: PathwaySubPathway/479683
pathway component: ReactionCatalysis1073233
pathway component: 2.7.7.24
pathway component: ReactionCatalysis1073234
pathway component: ReactionCatalysis1073231
pathway component: 2.6.1.59
pathway component: 2.3.1.210
pathway component: ReactionCatalysis1073232
pathway component: Amino Sugar and Nucleotide Sugar Metabolism I
pathway component: Galactose Degradation/Leloir Pathway
pathway component: ReactionCatalysis1073235
pathway component: Transport68663
pathway component: TransportCatalysis49193
pathway component: ReactionCatalysis1072931
pathway component: ReactionCatalysis1073229
pathway component: 2.4.1.325
pathway component: 2.4.1.180
pathway component: 2.7.8.33
pathway component: Secondary Metabolites: Methylerythritol Phosphate and Polyisoprenoid Biosynthesis
pathway component: ReactionCatalysis1073230
pathway component: 4.2.1.46
xref: Reference/PathWhiz PW460124
xref: Reference/SMPDB SMP0443884
organism: Bacteroides xylanisolvens XB1A

Reference/BioCyc C55-PP-GLCNAC-MANNACA
type: UnificationXref
id: C55-PP-GLCNAC-MANNACA
db: BioCyc

Reference/ChemSpider 6557
type: UnificationXref
id: 6557
db: ChemSpider

ChemicalStructure/PW C042941
type: ChemicalStructure
structure format: SMILES

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 53481400
xref: Reference/HMDB HMDB0012307
chemical formula: C79H129N3O22P2
molecular weight: 1533.8542
structure: ChemicalStructure/PW C007839

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate pyrophosphate
type: SmallMoleculeReference
xref: Reference/BioCyc C55-PP-GLCNAC-MANNACA
xref: Reference/HMDB HMDB0012306
xref: Reference/PubChem-compound 25245571
chemical formula: C71H116N2O18P2
molecular weight: 1346.7699
structure: ChemicalStructure/PW C007838

ChemicalStructure/PW C000940
type: ChemicalStructure
structure format: SMILES

Reference/CAS 7732-18-5
type: UnificationXref
id: 7732-18-5
db: CAS

Reference/ChEBI CHEBI 16077
type: UnificationXref
id: CHEBI:16077
db: ChEBI

Protein/55818/Stoichiometry/4.0
type: Stoichiometry
physical entity: Glucose-1-phosphate thymidylyltransferase
stoichiometric coefficient: 4.0

Compound/PW C007839 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
stoichiometric coefficient: 1.0

Reference/PubChem-compound 25245571
type: UnificationXref
id: 25245571
db: PubChem-compound

Reference/CAS 56-86-0
type: UnificationXref
id: 56-86-0
db: CAS

L-Glutamic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 33032
xref: Reference/ChEBI CHEBI 16015
xref: Reference/ChemSpider 30572
xref: Reference/HMDB HMDB0000148
xref: Reference/CAS 56-86-0
xref: Reference/BioCyc GLT
xref: Reference/KEGG Compound C00025
chemical formula: C5H9NO4
molecular weight: 147.05316
structure: ChemicalStructure/PW C000095

TDP-Fuc4NAc
type: SmallMoleculeReference
chemical formula: C18H29N3O15P2
molecular weight: 589.10736
structure: ChemicalStructure/PW C042652

Reference/PubChem-compound 33032
type: UnificationXref
id: 33032
db: PubChem-compound

UDP-ManNAcA
type: SmallMoleculeReference
chemical formula: C17H22N3O18P2
molecular weight: 618.03735
structure: ChemicalStructure/PW C042654

Compound/PW C001099/Stoichiometry/1.0
type: Stoichiometry
physical entity: Coenzyme A
stoichiometric coefficient: 1.0

dTDP-4-dehydro-6-deoxy-D-glucose
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0060081
chemical formula: C16H24N2O15P2
molecular weight: 546.0652
structure: ChemicalStructure/PW C042658

Reference/PubChem-compound 445675
type: UnificationXref
id: 445675
db: PubChem-compound

Transport68663
type: Transport
participant stoichiometry: Compound/PW C007839 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007839 Periplasmic Space/Stoichiometry/1.0
right: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
spontaneous: false
left: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
name: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate (→) Transport: Bacteroides xylanisolvens XB1A, Cytosol to Bacteroides xylanisolvens XB1A, Periplasmic Space
conversion direction: LEFT_TO_RIGHT

Reference/BioCyc UDP-N-ACETYL-D-GLUCOSAMINE
type: UnificationXref
id: UDP-N-ACETYL-D-GLUCOSAMINE
db: BioCyc

Compound/PW C000134/Stoichiometry/1.0
type: Stoichiometry
physical entity: Oxoglutaric acid
stoichiometric coefficient: 1.0

Reference/BioCyc DTDP-D-GLUCOSE
type: UnificationXref
id: DTDP-D-GLUCOSE
db: BioCyc

Reference/HMDB HMDB0000288
type: UnificationXref
id: HMDB0000288
db: HMDB

Reference/PubChem-compound 439324
type: UnificationXref
id: 439324
db: PubChem-compound

Compound/PW C001024/Stoichiometry/1.0
type: Stoichiometry
physical entity: dTDP-D-glucose
stoichiometric coefficient: 1.0

Compound/PW C042942/Stoichiometry/1.0
type: Stoichiometry
physical entity: dTDP-thomosamine
stoichiometric coefficient: 1.0

Reference/PubChem-compound 962
type: UnificationXref
id: 962
db: PubChem-compound

dTDP-thomosamine
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 68492
chemical formula: C16H26N3O14P2
molecular weight: 546.08954
structure: ChemicalStructure/PW C042942

N-acetyl-α-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 7137
chemical formula: C63H105NO12P2
molecular weight: 1129.7112
structure: ChemicalStructure/PW C042941

Reference/BioCyc 2-KETOGLUTARATE
type: UnificationXref
id: 2-KETOGLUTARATE
db: BioCyc

Reference/ChemSpider 392413
type: UnificationXref
id: 392413
db: ChemSpider

Reference/CAS 58-98-0
type: UnificationXref
id: 58-98-0
db: CAS

Reference/ChEBI CHEBI 18077
type: UnificationXref
id: CHEBI:18077
db: ChEBI

Reference/ChEBI CHEBI 18075
type: UnificationXref
id: CHEBI:18075
db: ChEBI

ChemicalStructure/PW C007839
type: ChemicalStructure
structure format: SMILES

Reference/ChEBI CHEBI 16695
type: UnificationXref
id: CHEBI:16695
db: ChEBI

Reference/SMPDB SMP0443884
type: UnificationXref
id: SMP0443884
db: SMPDB

di-trans,octa-cis-undecaprenyl phosphate
type: SmallMolecule
entity reference: di-trans,octa-cis-undecaprenyl phosphate
name: SubPathwayOutput

ChemicalStructure/PW C007838
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C00080
type: UnificationXref
id: C00080
db: KEGG Compound

Periplasmic Space
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005620

Oxoglutaric acid
type: SmallMolecule
entity reference: Oxoglutaric acid

Reference/HMDB HMDB0000290
type: UnificationXref
id: HMDB0000290
db: HMDB

Reference/HMDB HMDB0000295
type: UnificationXref
id: HMDB0000295
db: HMDB

ChemicalStructure/PW C000095
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCC(O)=O)C(O)=O

Reference/HMDB HMDB0002111
type: UnificationXref
id: HMDB0002111
db: HMDB

Protein/76734/Stoichiometry/2.0
type: Stoichiometry
physical entity: Phospho-N-acetylmuramoyl-pentapeptide-transferase
stoichiometric coefficient: 2.0

Reference/ChemSpider 5809
type: UnificationXref
id: 5809
db: ChemSpider

Reference/ChemSpider 5808
type: UnificationXref
id: 5808
db: ChemSpider

Reference/ChEBI CHEBI 15377
type: UnificationXref
id: CHEBI:15377
db: ChEBI

Reference/ChEBI CHEBI 15378
type: UnificationXref
id: CHEBI:15378
db: ChEBI

ChemicalStructure/PW C040034
type: ChemicalStructure
structure format: SMILES
structure data: [H+]

Glucose 1-phosphate
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001586
xref: Reference/PubChem-compound 439165
xref: Reference/CAS 59-56-3
xref: Reference/BioCyc GLC-1-P
xref: Reference/ChEBI CHEBI 16077
xref: Reference/KEGG Compound C00103
xref: Reference/ChemSpider 388311
chemical formula: C6H13O9P
molecular weight: 260.02972
structure: ChemicalStructure/PW C001207

Compound/PW C001420/Stoichiometry/1.0
type: Stoichiometry
physical entity: Water
stoichiometric coefficient: 1.0

Reference/CAS 2196-62-5
type: UnificationXref
id: 2196-62-5
db: CAS

Reference/HMDB HMDB0001274
type: UnificationXref
id: HMDB0001274
db: HMDB

Protein/55818 Cytosol/Stoichiometry/4.0
type: Stoichiometry
physical entity: Glucose-1-phosphate thymidylyltransferase
stoichiometric coefficient: 4.0

4.2.1.46
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042658/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001024/Stoichiometry/1.0
right: Water
right: dTDP-4-dehydro-6-deoxy-D-glucose
spontaneous: false
EC number: 4.2.1.46
left: dTDP-D-glucose
name: dTDP-D-glucose → Water + dTDP-4-dehydro-6-deoxy-D-glucose
conversion direction: LEFT_TO_RIGHT

Reference/CAS 491-97-4
type: UnificationXref
id: 491-97-4
db: CAS

Reference/SMPDB SMP0000903
type: UnificationXref
id: SMP0000903
db: SMPDB

Reference/PubChem-compound 644102
type: UnificationXref
id: 644102
db: PubChem-compound

Reference/PubChem-compound 444493
type: UnificationXref
id: 444493
db: PubChem-compound

dTDP-glucose 4,6-dehydratase
type: Protein
entity reference: dTDP-glucose 4,6-dehydratase

ChemicalStructure/PW C000987
type: ChemicalStructure
structure format: SMILES

Glucose 1-phosphate
type: SmallMolecule
entity reference: Glucose 1-phosphate

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate

Reference/SMPDB SMP0000905
type: UnificationXref
id: SMP0000905
db: SMPDB

ChemicalStructure/PW C000196
type: ChemicalStructure
structure format: SMILES

Glucose-1-phosphate thymidylyltransferase
type: ProteinReference
xref: Reference/UniProt D6D5T2

Reference/BioCyc ACETYL-COA
type: UnificationXref
id: ACETYL-COA
db: BioCyc

Water
type: SmallMoleculeReference
xref: Reference/PubChem-compound 962
xref: Reference/ChEBI CHEBI 15377
xref: Reference/KEGG Compound C00001
xref: Reference/ChemSpider 937
xref: Reference/HMDB HMDB0002111
xref: Reference/CAS 7732-18-5
chemical formula: H2O
molecular weight: 18.010565
structure: ChemicalStructure/PW C001420

Aspartate/tyrosine/aromatic aminotransferase
type: ProteinReference
xref: Reference/UniProt D6D4W8

SubPathwayInteraction479682
type: Interaction
name: SubPathwayReaction
name: SubPathway479682Reaction
participant: di-trans,octa-cis-undecaprenyl phosphate

SubPathwayInteraction479683
type: Interaction
name: SubPathway479683Reaction
name: SubPathwayReaction
participant: dTDP-glucose pyrophosphorylase 2

ChemicalStructure/PW C000194
type: ChemicalStructure
structure format: SMILES

SubPathwayInteraction479681
type: Interaction
name: SubPathwayReaction
name: SubPathway479681Reaction
participant: UDP-ManNAcA

Reference/TAXONOMY 657309
type: UnificationXref
id: 657309
db: TAXONOMY

Compound/PW C001207/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucose 1-phosphate
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 17659
type: UnificationXref
id: CHEBI:17659
db: ChEBI

Reference/HMDB HMDB0059597
type: UnificationXref
id: HMDB0059597
db: HMDB

Reference/BioCyc UMP
type: UnificationXref
id: UMP
db: BioCyc

TransportCatalysis49193
type: Catalysis
controller: Membrane protein involved in the export of O-antigen and teichoic acid
controlled: Transport68663
control type: ACTIVATION

di-trans,octa-cis-undecaprenyl phosphate
type: SmallMoleculeReference
chemical formula: C55H91O4P
molecular weight: 846.6655
structure: ChemicalStructure/PW C042617

dTDP-glucose pyrophosphorylase 2
type: Complex
component stoichiometry: Protein/55818 Cytosol/Stoichiometry/4.0
cellular location: Cytosol
component: Glucose-1-phosphate thymidylyltransferase

Reference/ChEBI CHEBI 15351
type: UnificationXref
id: CHEBI:15351
db: ChEBI

Compound/PW C001207 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucose 1-phosphate
stoichiometric coefficient: 1.0

Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate
type: SmallMolecule
cellular location: Periplasmic Space
entity reference: Undecaprenyl N-acetyl-glucosaminyl-N-acetyl-mannosaminuronate-4-acetamido-4,6-dideoxy-D-galactose pyrophosphate

Reference/CAS 85-61-0
type: UnificationXref
id: 85-61-0
db: CAS